| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:101281792-101281845 | Rare:9 | ||||
| chr15:101289129-101289417 | Common:2; Rare:49 | ||||
| chr16:192311-192370 | Rare:13 | ||||
| chr16:399349-399736 | Common:4; Rare:155 | ||||
| chr16:400742-400863 | Common:2; Rare:26 | ||||
| chr16:580864-581048 | Common:1; Rare:73; Clinvar:6; Clinvar (benign):2 | ||||
| chr16:634687-635188 | Rare:165 | ||||
| chr16:679362-679525 | Common:2; Rare:43 | ||||
| chr16:857900-858122 | Common:1; Rare:9 | ||||
| chr16:1362870-1363062 | Rare:101; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr16:1408187-1408418 | Common:6; Rare:97 | ||||
| chr16:1828001-1828210 | Common:3; Rare:40 | ||||
| chr16:1939102-1939311 | Common:1; Rare:67 | ||||
| chr16:2154846-2154915 | Rare:14 | ||||
| chr16:2156481-2156643 | Common:2; Rare:31 |